Nils-Ake has over 30 years of experience in the medical device industry. He has long management experience in Quality Assurance and Regulatory Affairs but also senior management positions within production, technical services, and development. Nils-Ake provides support for management as well as line staff in a multitude of aspects to both large corporations and start-ups. It may be regulatory strategies or compliance projects on both local and corporate levels. Nils-Ake holds an MSc in Electrical/Biomedical Engineering. He is a board member of the European Association of Authorised Representatives (EAAR) and participates in the EU commission working group. Active member in SIS/TK355, and TC201/WG1 standard committee for Medical Quality Systems. CEO of QAdvis.
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